Canonical Allele Identifier: CA298974

Gene: CDH1

Linked Data

• ClinVar Variation Id: 182393
• ClinVar RCV Id: RCV000160385
• dbSNP Id: rs730881663
• MyVariant Identifiers: chr16:g.68844119C>A (hg19) ; chr16:g.68810216C>A (hg38)
• ERepo: CA298974/MONDO:0007648/007 ; CA298974/MONDO:0100488/007

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810216C>A , CM000678.2:g.68810216C>A	GRCh38
NC_000016.9:g.68844119C>A , CM000678.1:g.68844119C>A	GRCh37
NC_000016.8:g.67401620C>A	NCBI36
NG_008021.1:g.77925C>A , LRG_301:g.77925C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.707C>A MANE Select	ENSP00000261769.4:p.Ser236Ter
ENST00000261769.9:c.707C>A	ENSP00000261769.4:p.Ser236Ter
ENST00000422392.6:c.707C>A	ENSP00000414946.2:p.Ser236Ter
ENST00000561751.1:c.454+1368C>A
ENST00000562836.5:n.778C>A
ENST00000566510.5:c.551C>A	ENSP00000458139.1:p.Ser184Ter
ENST00000566612.5:c.707C>A	ENSP00000454782.1:p.Ser236Ter
ENST00000611625.4:c.707C>A	ENSP00000481063.1:p.Ser236Ter
ENST00000612417.4:c.707C>A	ENSP00000478360.1:p.Ser236Ter
ENST00000621016.4:c.707C>A	ENSP00000480664.1:p.Ser236Ter
NM_004360.3:c.707C>A , LRG_301t1:c.707C>A	NP_004351.1:p.Ser236Ter
XM_011523488.1:c.-29C>A	XP_011521790.1:n.-29C>A
XM_011523489.1:c.-29C>A	XP_011521791.1:n.-29C>A
NM_001317184.1:c.707C>A	NP_001304113.1:p.Ser236Ter
NM_001317185.1:c.-909C>A	NP_001304114.1:n.-909C>A
NM_001317186.1:c.-1113C>A	NP_001304115.1:n.-1113C>A
NM_004360.4:c.707C>A	NP_004351.1:p.Ser236Ter
NM_004360.5:c.707C>A MANE Select	NP_004351.1:p.Ser236Ter
NM_001317184.2:c.707C>A	NP_001304113.1:p.Ser236Ter
NM_001317185.2:c.-909C>A	NP_001304114.1:n.-909C>A
NM_001317186.2:c.-1113C>A	NP_001304115.1:n.-1113C>A